Rapid seasonal adaptation of an alien bruchid after introduction: geographic variation in life cycle synchronization and critical photoperiod for diapause induction

2011 ◽  
Vol 140 (1) ◽  
pp. 69-76 ◽  
Author(s):  
Shou Sadakiyo ◽  
Michihiro Ishihara
Keyword(s):  
Life Cycle ◽  
Geographic Variation ◽  
Diapause Induction ◽  
Seasonal Adaptation ◽  
Critical Photoperiod

scholarly journals Geographic Variation in Diapause Induction: The Grape Berry Moth (Lepidoptera: Tortricidae)

2010 ◽  
Vol 39 (6) ◽  
pp. 1751-1755 ◽  
Author(s):  
Jody Timer ◽  
Patrick C. Tobin ◽  
Michael C. Saunders
Keyword(s):  
Geographic Variation ◽  
Grape Berry ◽  
Diapause Induction

Phenology and seed production in Chenopodium rubrum, Rumex maritimus, and Rumex palustris as related to photoperiod in river forelands

1992 ◽  
Vol 70 (2) ◽  
pp. 392-400 ◽  
Author(s):  
A. J. M. Van der Sman ◽  
C. W. P. M. Blom ◽  
H. M. Van de Steeg
Keyword(s):  
Life Cycle ◽  
Seed Production ◽  
Population Level ◽  
Flowering Phenology ◽  
Chenopodium Rubrum ◽  
Axillary Shoots ◽  
Critical Photoperiod ◽  
Number Of Leaves ◽  
Rumex Maritimus ◽  
Flooded Areas

Reproductive development in three species from irregularly flooded areas of river forelands was studied in relation to time of emergence. In Chenopodium rubrum, flowering was induced earlier in plants germinated in April–May than in later cohorts. However, the period of vegetative growth diminished and the life cycle was completed in a shorter time in later germinated plants. Seed number was reduced, but seed size as well as reproductive effort per plant increased in later cohorts. Plants of both Rumex species flowered after a certain number of leaves had developed and before a critical photoperiod had passed. In earlier cohorts, the main shoot and several axillary shoots elongated and flowered. Fewer axillary shoots flowered closer to the critical photoperiod, and this resulted in a reduced seed output in later cohorts. The critical photoperiod as well as the time needed for completion of the life cycle was longer in Rumex palustris than in Rumex maritimus. It is argued that in the riparian habitat, plants of both Rumex species are only occasionally able to complete their life cycle in one growing season. Survival of these species on the population level will rely more upon adaptations towards flooding during the established phase than is the case for C. rubrum. Key words: flowering phenology, photoperiod, seed production, Chenopodium rubrum, Rumex maritimus, Rumex palustris.

scholarly journals Reproductive diapause in Nysius huttoni White (Heteroptera Lygaeidae)

2002 ◽  
Vol 55 ◽  
pp. 308-311
Author(s):  
X.Z. He ◽  
Q. Wang ◽  
A. Carpenter
Keyword(s):  
Life Cycle ◽  
Immature Stages ◽  
Life Stages ◽  
Reproductive Diapause ◽  
Entire Life ◽  
Entire Life Cycle ◽  
Adult Females ◽  
Critical Photoperiod

The induction of reproductive diapause of Nysius huttoni was studied in the laboratory at 20 1C and 60 10 RH under a series of photoperiod regimes 168 h 1410 h 1212 h and 1014 h lightdark Reproductive diapause was considered to have occurred if females failed to lay eggs for 50 days after emergence The sensitivity of different life stages to diapauseinducing photoperiods varied When newly emerged females whose immature stages had been reared at 168 h were transferred to 1014 h and 1212 h 467 and 793 of them entered reproductive diapause respectively However when fifth instar nymphs were transferred from 168 h to 1014 h and 1212 h 100 of adult females entered reproductive diapause If the entire life cycle was maintained at 1014 h and 1212 h 667 and 400 of females entered reproductive diapause respectively The critical photoperiod for reproductive diapause was estimated to lie between 1311 h and 135105 h

EFFECT OF LATITUDE ON THE CRITICAL PHOTOPERIOD FOR DIAPAUSE INDUCTION IN THE BERTHA ARMYWORM, MAMESTRA CONFIGURATA (LEPIDOPTERA: NOCTUIDAE)

1983 ◽  
Vol 115 (8) ◽  
pp. 1039-1042 ◽  
Author(s):  
B. M. Hegdekar
Keyword(s):  
Temperature Regime ◽  
Diapause Induction ◽  
The Other ◽  
Fluctuating Temperature ◽  
Mamestra Configurata ◽  
Ambient Temperatures ◽  
Critical Photoperiod ◽  
Lepidoptera Noctuidae ◽  
H 20 ◽  
Bertha Armyworm

AbstractThe critical photoperiod for diapause induction in pupae of Mamestra configurata Walker in Manitoba was 16 h 06 min at Glenlea (49°38′ N), 16 h 20 min at Grandview (51°10′ N), and 16 h 42 min at Birch River (52°24′ N). The differences in cirtical photoperiods observed at Glenlea and Grandview were not significant. At least two different photoperiods exist, one in the Glenlea and Grandview areas and the other in the Birch River area. In the laboratory, the critical photoperiod was 13.5 h when larvae were exposed to a daily fluctuating temperature regime of 12 h at 25 °C and 12 h at 10 °C. Longer critical photoperiods found for the field populations may be related to the relatively low ambient temperatures to which the larvae were exposed in field cages.

Diapause Induction in a Kentucky Population of Diprion similis (Hymenoptera: Diprionidae)

1999 ◽  
Vol 34 (3) ◽  
pp. 328-334 ◽  
Author(s):  
Heidi L. Melcher ◽  
Lee H. Townsend
Keyword(s):  
Diapause Induction ◽  
Pine Sawfly ◽  
Sensitive Stage ◽  
Diprion Similis ◽  
Critical Photoperiod ◽  
Photoperiod Sensitive ◽  
Chilling Period

Critical photoperiod, sensitive stage for diapause induction, and requirements for termination of diapause were studied in a colony of the introduced pine sawfly, Diprion similis (Hartig), established from a feral Kentucky population. We investigated induction of diapause in the laboratory under photoperiods of 10:14, 11:13, 12:12, 13:11, 14:10, 15:9, and 16:8 (L:D) in the first trial, and added a photoperiod of 9:15 (L:D) in the second trial. Individuals exposed to light periods ≤12:12 (L:D) entered diapause; individuals in a photoperiod > 13:11 (L:D) bypassed diapause. The sensitive stage was determined using reciprocal switches of diapause-inducing (9:15) and non-diapause inducing (16:8) L:D regimes. Our studies indicated that late instars of the introduced pine sawfly are significantly sensitive to photoperiod. Termination of diapause in D. similis did not require a cold or chilling period. All individuals from critical photoperiod trials were kept at 22°C to determine the duration of diapause. Diapausing individuals emerged from the cocoon after 82 to 105 d, compared to 6 to 23 d for individuals not entering diapause.

THERMAL ACCUMULATIONS, DIAPAUSE, AND OVIPOSITION IN A CONIFER-INHABITING PREDATOR, CHRYSOPA HARRISII (NEUROPTERA)

1974 ◽  
Vol 106 (9) ◽  
pp. 969-978 ◽  
Author(s):  
Maurice J. Tauber ◽  
Catherine A. Tauber
Keyword(s):  
Diapause Induction ◽  
Temperature Threshold ◽  
Heat Accumulation ◽  
Species Occurrence ◽  
Winter Solstice ◽  
Critical Photoperiod ◽  
Diapause Development ◽  
Dark Green ◽  
Active Adults ◽  
Short Days

AbstractThe adults of Chrysopa harrisii Fitch, which are not predaceous, overwinter in a state of reproductive diapause. During both the dormant and the reproductive periods they remain dark green, a colour apparently adapted to the species’ occurrence on conifers. Two to three generations per season are possible in the Ithaca, N.Y., area.At 75°F, which is the optimum constant temperature for development and survival, the time from oviposition to adult eclosion is 29 days. Theoretical thresholds for development of all stages are relatively high, between 50° and 57°F, and development from egg to adult requires 566 heat degree days.In the laboratory, the critical photoperiod for diapause induction is between LD 13:11 and LD 14:10; short days maintain diapause for approximately 45 days (at 75°F); long days terminate diapause. Both newly-emerged and reproductively-active adults are extremely sensitive to diapause-inducing photoperiods. In the field, all adults emerging on 5 September or later enter diapause and it appears that diapause induction in the Ithaca population begins in the latter part of August. Short days maintain diapause until the end of December, and neither long days, increasing day lengths, nor low temperatures play a role in hastening diapause termination in nature.In timing its vernal reproduction, C. harrisii has evolved a strategy that combines an early-ending diapause with an apparently relatively high temperature threshold for post-diapause development. Therefore, although diapause ends around the winter solstice, heat accumulation is prevented until much later, when temperatures are relatively high.

scholarly journals Geographic Variation of Diapause Induction and Termination in the Spider Mite Tetrαnychus urticαe: Α mini-review

2017 ◽  
Vol 12 ◽  
pp. 5 ◽  
Author(s):  
S. Koveos ◽  
A. Veerman
Keyword(s):  
Geographic Variation ◽  
Spider Mite ◽  
Wide Distribution ◽  
Mite Species ◽  
Climatic Conditions ◽  
Diapause Induction ◽  
Diapause Termination ◽  
Long Day ◽  
Critical Daylength ◽  
Tetranychus Urticae Koch

In eight strains of the spider mite Tetranychus urticae Koch (Acari: Tetranychidae), originating from different localities in Europe, the critical daylength for diapause induction and termination was almost the same in each strain but varied with the latitudinal origin of the strains; critical daylength was shorter in strains originating from lower latitudes and longer in those from higher latitudes. Diapause intensity, measured as the period of chilling required for diapause termination under a short day photoperiod (LD 10:14) and 19°C, again varied with the latitudinal origin of each strain, being higher the more northern the origin of the strain. An exception were two mountain strains which showed a longer critical daylength and a deeper diapause than expected on the basis of their latitudinal origin. The number of long-day (LD 17:7) cycles required for 50% diapause termination after a certain period of chilling was higher in the northern and lower in the southern strains. These results indicate that geographic strains of T urticae may differ considerably in their diapause attributes, which may be explained as an adaptation to local climatic conditions. The great plasticity of the diapause response may, among other factors, have been responsible for the wide distribution of this mite species.

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